| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:9749915-9750249 | Common:2; Rare:77 | ||||
| chr19:10173873-10173935 | Rare:17 | ||||
| chr19:10581263-10581490 | Common:4; Rare:91 | ||||
| chr19:10581628-10581768 | Rare:47 | ||||
| chr19:10634969-10635230 | Common:2; Rare:76 | ||||
| chr19:10640109-10640399 | Common:5; Rare:58 | ||||
| chr19:11027619-11027805 | Rare:47; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:11111287-11111636 | Common:4; Rare:98; Clinvar:18; Clinvar (benign):1; Clinvar (pathogenic):11 | ||||
| chr19:11123000-11123343 | Common:5; Rare:96; Clinvar:10; Clinvar (benign):10; Clinvar (pathogenic):6 | ||||
| chr19:11335505-11335762 | Common:1; Rare:96 | ||||
| chr19:11522401-11522539 | Rare:20 | ||||
| chr19:11737587-11737770 | Common:1; Rare:25 | ||||
| chr19:11835396-11835413 | Rare:3 | ||||
| chr19:12403580-12403730 | Common:1; Rare:34 | ||||
| chr19:12710650-12710868 | Rare:55 |